ClearanceBrief
Company ยท US

Amerimed US Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1988 to 1989. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
LYYLatex Patient Examination Glove3
LBKNeurosurgical Ultrasonic Instruments1
LYZVinyl Patient Examination Glove1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jul 14, 1989K891722LATEX EXAM GLOVES (MFG. SHANGHAI MEHECO)
Amerimed US Corp.
LYY
May 31, 1989K891437PATIENT EXAMINATION GLOVES (LATEX)
Amerimed US Corp.
LYY
May 31, 1989K891436PATIENT EXAMINATION GLOVES (LATEX)
Amerimed US Corp.
LYY
May 4, 1989K890967VINYL EXAMINATION GLOVES (MFG. SALZGITTER MOREX)
Amerimed US Corp.
LYZ
Sep 30, 1988K883522AMERIMED ULTRASONIC SURGICAL ASPIRATION KIT
Amerimed US Corp.
LBK

Latest recalls

DateFirm and productCodeLinked 510(k)
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